U.S. flag An official website of the United States government
  1. Home
  2. Drug Databases
  3. Orange Book Home

Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

Home | Back to Search Results

Product Details for ANDA 202360

ETOMIDATE (ETOMIDATE)
2MG/ML
Marketing Status: Prescription
Active Ingredient: ETOMIDATE
Proprietary Name: ETOMIDATE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 2MG/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A202360
Product Number: 001
Approval Date: Jul 18, 2014
Applicant Holder Full Name: ZYDUS PHARMACEUTICALS USA INC
Marketing Status:  Prescription
Patent and Exclusivity Information
Back to Top